510(k) Report

Devices descending from K030931

13 later devices reach C3 Patient Monitor through their predicates, nearest generation first.

GenerationNumberDeviceApplicantDecidedOwn descendantsRecalls
+1K051903Fetalgard Lite-Nibp, Model FGL-NibpAnalogic Corporation20050—
+1K050919Lifegard II Family Multi-Function Patient Monitor, Models AN4320, AN4320P, AN4321P…Analogic Corp.20050—
+1K041434C3 and Lifegard Icg Impedance Cardiography MonitorsAnalogic Corp.200411—
+2K060387Physioflow SystemVasocom, Inc.20084—
+2K070156Bioz DX Hemodynamic Monitor with Philips 12-Lead Ecg, Model 5100Cardiodynamics International Corp.20074—
+3K160899CoVa Monitoring System 2Tosense, Inc.20170—
+3K103283Physioflow EnduroVasocom, Inc.20103—
+3K080941Bioimpedance Cardiac Analyzing Measuring SystemN.I. Medical, Ltd.20090—
+3K090602Cardiodynamics Bioz RX, Model 7101-SysCardiodynamics International Corp.20091—
+4K140102Physioflow Q-LinkVasocom, Inc.20142—
+4K110645Bio Z Cardio Profile Hemodynamic MonitorSonosite,Inc.20110—
+5K172457Deltex Medical CardioQ-EDM+, Deltex Medical CardioQ-EDMDeltex Medical Limited20180—
+5K173156Integrated CardioRespiratory SystemSensydia, Inc.20180—